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1000 results for “organic_chemistry”
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Novel enantioselective #synthesis of rubriflordilactone B by Gui and colleagues from the Chinese Academy of Science published in #JACS
This is already the second total synthesis of this group, with an interesting reaction cascade as the key reaction in this process. -
Novel enantioselective #synthesis of rubriflordilactone B by Gui and colleagues from the Chinese Academy of Science published in #JACS
This is already the second total synthesis of this group, with an interesting reaction cascade as the key reaction in this process. -
Novel enantioselective #synthesis of rubriflordilactone B by Gui and colleagues from the Chinese Academy of Science published in #JACS
This is already the second total synthesis of this group, with an interesting reaction cascade as the key reaction in this process. -
Novel enantioselective #synthesis of rubriflordilactone B by Gui and colleagues from the Chinese Academy of Science published in #JACS
This is already the second total synthesis of this group, with an interesting reaction cascade as the key reaction in this process. -
Luo et al. from Tsinghua University (#China) report in #JACS a novel method to create enantioenriched α-amino aldehydes using a chiral amine catalyst and iridium photocatalysis. Through this strategy α-amino aldehydes with up to 93% ee could be synthesised and subsequently stabilised via analogues formation (e.g. through Wittig reaction).
https://me.organicchemistry.eu/post/deracemization-aldehyde-jacs-2025/
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Luo et al. from Tsinghua University (#China) report in #JACS a novel method to create enantioenriched α-amino aldehydes using a chiral amine catalyst and iridium photocatalysis. Through this strategy α-amino aldehydes with up to 93% ee could be synthesised and subsequently stabilised via analogues formation (e.g. through Wittig reaction).
https://me.organicchemistry.eu/post/deracemization-aldehyde-jacs-2025/
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Luo et al. from Tsinghua University (#China) report in #JACS a novel method to create enantioenriched α-amino aldehydes using a chiral amine catalyst and iridium photocatalysis. Through this strategy α-amino aldehydes with up to 93% ee could be synthesised and subsequently stabilised via analogues formation (e.g. through Wittig reaction).
https://me.organicchemistry.eu/post/deracemization-aldehyde-jacs-2025/
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Luo et al. from Tsinghua University (#China) report in #JACS a novel method to create enantioenriched α-amino aldehydes using a chiral amine catalyst and iridium photocatalysis. Through this strategy α-amino aldehydes with up to 93% ee could be synthesised and subsequently stabilised via analogues formation (e.g. through Wittig reaction).
https://me.organicchemistry.eu/post/deracemization-aldehyde-jacs-2025/
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Joseph Tuccinardi and John Wood from Baylor University (#USA), introduced a novel strategy to efficiently synthesize the core scaffold of aleutianamine. Their study involved a vinylogous Mukaiyama-Michael reaction cascade using two previously unknown coupling partners. Published in #JACS
https://me.organicchemistry.eu/post/aleutianamine-jacs-2025/
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Joseph Tuccinardi and John Wood from Baylor University (#USA), introduced a novel strategy to efficiently synthesize the core scaffold of aleutianamine. Their study involved a vinylogous Mukaiyama-Michael reaction cascade using two previously unknown coupling partners. Published in #JACS
https://me.organicchemistry.eu/post/aleutianamine-jacs-2025/
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Joseph Tuccinardi and John Wood from Baylor University (#USA), introduced a novel strategy to efficiently synthesize the core scaffold of aleutianamine. Their study involved a vinylogous Mukaiyama-Michael reaction cascade using two previously unknown coupling partners. Published in #JACS
https://me.organicchemistry.eu/post/aleutianamine-jacs-2025/
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Joseph Tuccinardi and John Wood from Baylor University (#USA), introduced a novel strategy to efficiently synthesize the core scaffold of aleutianamine. Their study involved a vinylogous Mukaiyama-Michael reaction cascade using two previously unknown coupling partners. Published in #JACS
https://me.organicchemistry.eu/post/aleutianamine-jacs-2025/
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Another total synthesis in the spotlight: Already early this year Mingji Dai and his research team described the total synthesis of heilonine in #JACS (doi: 10.1021/jacs.3c13492). This synthesis is short and elegant, using multiple C-H functionalisations and a Nazarov cyclisation for their key step.
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Another total synthesis in the spotlight: Already early this year Mingji Dai and his research team described the total synthesis of heilonine in #JACS (doi: 10.1021/jacs.3c13492). This synthesis is short and elegant, using multiple C-H functionalisations and a Nazarov cyclisation for their key step.
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Another total synthesis in the spotlight: Already early this year Mingji Dai and his research team described the total synthesis of heilonine in #JACS (doi: 10.1021/jacs.3c13492). This synthesis is short and elegant, using multiple C-H functionalisations and a Nazarov cyclisation for their key step.
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Another total synthesis in the spotlight: Already early this year Mingji Dai and his research team described the total synthesis of heilonine in #JACS (doi: 10.1021/jacs.3c13492). This synthesis is short and elegant, using multiple C-H functionalisations and a Nazarov cyclisation for their key step.
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The construction of quaternary centres via C-C bond formation is a major challenge. A new stereoselective method using lithium enolates and Ru-catalysed allylic substitution has been reported in #JACS by the group of Erick Carreira (ETH #Zürich). This promising approach provides access to these sterically crowded motifs.
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The construction of quaternary centres via C-C bond formation is a major challenge. A new stereoselective method using lithium enolates and Ru-catalysed allylic substitution has been reported in #JACS by the group of Erick Carreira (ETH #Zürich). This promising approach provides access to these sterically crowded motifs.
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The construction of quaternary centres via C-C bond formation is a major challenge. A new stereoselective method using lithium enolates and Ru-catalysed allylic substitution has been reported in #JACS by the group of Erick Carreira (ETH #Zürich). This promising approach provides access to these sterically crowded motifs.
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The construction of quaternary centres via C-C bond formation is a major challenge. A new stereoselective method using lithium enolates and Ru-catalysed allylic substitution has been reported in #JACS by the group of Erick Carreira (ETH #Zürich). This promising approach provides access to these sterically crowded motifs.
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📢 Invitation to submit!
New thematic issue “Novel #macrocycles: from synthesis to #supramolecular function” edited by Prof. Pablo Ballester, Konrad Tiefenbacher, Carmine Gaeta, Carmen Talotta, Margherita De Rosa and Paolo Della Sala in the Beilstein Journal of Organic Chemistry:
➡️ https://www.beilstein-journals.org/bjoc/series/142?M=ySubmission deadline 📅 March 31, 2025
#SupramolecularChemistry #catalysis #mechanomolecules #BJOC 💎🔓
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📢 Invitation to submit!
New thematic issue “Novel #macrocycles: from synthesis to #supramolecular function” edited by Prof. Pablo Ballester, Konrad Tiefenbacher, Carmine Gaeta, Carmen Talotta, Margherita De Rosa and Paolo Della Sala in the Beilstein Journal of Organic Chemistry:
➡️ https://www.beilstein-journals.org/bjoc/series/142?M=ySubmission deadline 📅 March 31, 2025
#SupramolecularChemistry #catalysis #mechanomolecules #BJOC 💎🔓
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📢 Invitation to submit!
New thematic issue “Novel #macrocycles: from synthesis to #supramolecular function” edited by Prof. Pablo Ballester, Konrad Tiefenbacher, Carmine Gaeta, Carmen Talotta, Margherita De Rosa and Paolo Della Sala in the Beilstein Journal of Organic Chemistry:
➡️ https://www.beilstein-journals.org/bjoc/series/142?M=ySubmission deadline 📅 March 31, 2025
#SupramolecularChemistry #catalysis #mechanomolecules #BJOC 💎🔓
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📢 Invitation to submit!
New thematic issue “Novel #macrocycles: from synthesis to #supramolecular function” edited by Prof. Pablo Ballester, Konrad Tiefenbacher, Carmine Gaeta, Carmen Talotta, Margherita De Rosa and Paolo Della Sala in the Beilstein Journal of Organic Chemistry:
➡️ https://www.beilstein-journals.org/bjoc/series/142?M=ySubmission deadline 📅 March 31, 2025
#SupramolecularChemistry #catalysis #mechanomolecules #BJOC 💎🔓
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Coming up on Thursday 📅 Jan 29, 2026 at 🕒 3 pm CET: Online #BeilsteinTalk “Bioinspired redox catalysis for synthetic challenges and sustainable chemistry” with Marine Desage-El Murr, University of Strasbourg.
Register for FREE 🔗 https://www.beilstein-institut.de/en/talks/organic-chemistry-bioinspired-redox-catalysis-for-synthetic-challenges-and-sustainable-chemistry/?M=y
#RedoxCatalysis #GreenChemistry #SustainableChemistry #BioinspiredCatalysis #BeilsteinTalks
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Coming up on Thursday 📅 Jan 29, 2026 at 🕒 3 pm CET: Online #BeilsteinTalk “Bioinspired redox catalysis for synthetic challenges and sustainable chemistry” with Marine Desage-El Murr, University of Strasbourg.
Register for FREE 🔗 https://www.beilstein-institut.de/en/talks/organic-chemistry-bioinspired-redox-catalysis-for-synthetic-challenges-and-sustainable-chemistry/?M=y
#RedoxCatalysis #GreenChemistry #SustainableChemistry #BioinspiredCatalysis #BeilsteinTalks
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Coming up on Thursday 📅 Jan 29, 2026 at 🕒 3 pm CET: Online #BeilsteinTalk “Bioinspired redox catalysis for synthetic challenges and sustainable chemistry” with Marine Desage-El Murr, University of Strasbourg.
Register for FREE 🔗 https://www.beilstein-institut.de/en/talks/organic-chemistry-bioinspired-redox-catalysis-for-synthetic-challenges-and-sustainable-chemistry/?M=y
#RedoxCatalysis #GreenChemistry #SustainableChemistry #BioinspiredCatalysis #BeilsteinTalks
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Coming up on Thursday 📅 Jan 29, 2026 at 🕒 3 pm CET: Online #BeilsteinTalk “Bioinspired redox catalysis for synthetic challenges and sustainable chemistry” with Marine Desage-El Murr, University of Strasbourg.
Register for FREE 🔗 https://www.beilstein-institut.de/en/talks/organic-chemistry-bioinspired-redox-catalysis-for-synthetic-challenges-and-sustainable-chemistry/?M=y
#RedoxCatalysis #GreenChemistry #SustainableChemistry #BioinspiredCatalysis #BeilsteinTalks
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Coming up next week: Online #BeilsteinTalk “Bioinspired redox catalysis for synthetic challenges and sustainable chemistry” with Marine Desage-El Murr, University of Strasbourg.
📅 Jan 29, 2026 🕒 3–4 pm CET
Participation is FREE – just register 🔗 https://www.beilstein-institut.de/en/talks/organic-chemistry-bioinspired-redox-catalysis-for-synthetic-challenges-and-sustainable-chemistry/?M=y
#RedoxCatalysis #GreenChemistry #SustainableChemistry #BioinspiredCatalysis #BeilsteinTalks
-
Coming up next week: Online #BeilsteinTalk “Bioinspired redox catalysis for synthetic challenges and sustainable chemistry” with Marine Desage-El Murr, University of Strasbourg.
📅 Jan 29, 2026 🕒 3–4 pm CET
Participation is FREE – just register 🔗 https://www.beilstein-institut.de/en/talks/organic-chemistry-bioinspired-redox-catalysis-for-synthetic-challenges-and-sustainable-chemistry/?M=y
#RedoxCatalysis #GreenChemistry #SustainableChemistry #BioinspiredCatalysis #BeilsteinTalks